Abstract: Paleontological exploration in the Turkana Basin near Ileret, Kenya yielded the most complete adult elephant cranium (KNM-ER 63642) known from the late Miocene to mid-Pliocene. KNM-ER 63642 derives from the lower Lonyumun Mb. of the Koobi Fora Fm. and dates to the early Pliocene, >4.3 Ma. The cranium is immense in size and preserves most of its structures including left and right M2-3, permitting its comprehensive comparative study and secure taxonomic assignment to Loxodonta adaurora. Features distinctive of the species and exhibited by KNM-ER 63642 include very elongate, divergent tusk alveoli, a short, biconvex cranial roof, anterosuperior angulation of the occipital planum, non-inflated occipital planum and absence of supralateral parietal "bossing," broad, flat premaxillary nasal processes, broad, laterally downturned nasal aperture superior to the level of the orbits, and M3s with wide, subhypsodont plates that are parallel-faced and separated by U-shaped transverse valleys. The M3s also exhibit characteristic L. adaurora traits of greatest width at their bases, rounded cross-sectional shape, thick enamel, abundant cementum, and strong anterior and posterior accessory conules. Of extant taxa, KNM-ER 63642 most closely resembles crania of African elephants. Its inclusion in the Loxodonta clade is tenuous, however, because shared features are either symplesiomorphic or are difficult to test for synapomorphy due to the poor fossil record of crania of late Miocene-early Pliocene elephants. Overall, the cranial morphology of KNM-ER 63642 is unexpectedly advanced for an elephant of its antiquity. Its anteroposterior compression and height are concordant with efficient proal masticatory action, indicating that by the early Pliocene L. adaurora evolved craniodental adaptations in phase with feeding preference for C4 grasses. The advantage of synchrony of morphology and behavior is reflected by the dominance of the species in the greater Turkana Basin during that interval.
  

Paleosols and the taphonomy of vertebrate fossils in the Eocene Kuldana Formation of northern Pakistan provide important information on the preservation and time-averaging of fossil assemblages. Morphologic, mineralogic, and chemical data as well as comparisons with Quaternary soils suggest that Kuldana paleosols formed under generally dry and oxidizing conditions over time intervals of less than 100 000 years and perhaps as short as 1000 years. The distribution of carbonate in Kuldana paleosols further indicates that the upper half of the profiles were acidic whereas the lower halves were alkaline. Vertebrate fossils are rare in Kuldana paleosols and occur primarily in well-cemented sandstones and conglomerates with abundant micritic and iron-stained nodules that were reworked from floodplain soils. The scarcity of vertebrate remains in Kuldana paleosols probably reflects a combination of acidic, dry, and oxidizing conditions in the upper half of the profiles and rapid floodplain sedimentation. Comparisons between the taphonomic characteristics of Kuldana channel fossil assemblages and bone accumulations in modem rivers provide a basis for estimating the length of time represented by Kuldana fossils from several important localities. Vertebrate fossil assemblages from Barbora Banda are characterized by a low-diversity paleofauna, partially articulated skeletons, and bones that are sorted by size and shape. Comparison with bone accumulations in modern rivers suggests that the fossils from Barbora Banda accumulated in 1 to 10 years. Vertebrate fossils from the Lower Kuldana in the Kala Chitta Hills region, typified by locality H-GSP 62, are characterized by a high-diversity paleofauna and generally random and unsorted fossil bone distributions, which suggest that the fossils from these localities represent longer time intervals than the Barbora Banda fossils. Based on the time estimates for Kuldana paleosol development, fossil assemblages in Kuldana channel deposits in the Kala Chitta Hills region probably represent time intervals of about 1000 years. 

The investigations undertaken at Crivadia (Hateg Depression, Hunedoara District, Romania), the type locality of Crivadiatherium mackennai RADULESCO el al. (Radulesco, Iliesco et lliesco, 1976), led to the discovery of remains of a new Embrithopod. Close to the above mentioned species, but larger in size, this animal is here described as a new species of Crivadiatherium, C. iliescui. ln addition, the comparison made between the forms indicated above and Palaeaamasía kansui OZANSOY from the Eocene deposits of Anatolia (Ozansoy, 1966; Sen et Heintz, 1979) showed that the latter species included a heterogeneous material; this permitted us to distinguish the form in the Anatolian locality Ciçekdag-Arabin Kôyü under the name Palaeoamasia sp. The geographical distribution and diversity of the Embrithopod species under discussion (Balkan, Anatolia) support the idea of an eurasiatic origin of this group and seem to suggest the existence during the Eocene of a particular faunal province in south-eastern Europe. 

L'exploitation des phosphates s'est produite surtout de 1890 à 1914 de Saint-Antonin à Cajarc, sur le Causse de Limogne, dont l'histoire géologique et morphologique peut expliquer les conditions de gisement du minerai, et aussi la découverte des nombreux, variés et beaux fossiles qu'on a extrait des poches en même temps que la phosphorite. Le Causse de Limogne est le nom donné par les géographes au plateau calcaire, faisant partie des Causses du Quercy, et compris entre la vallée du Lot au Nord et celle de "Aveyron au Sud". En fait, le nom de "causse" désigne localement un terroir, un paysage, à sous-sol de calcaire, à sol peu épais, qui s'oppose aux sols argileux des « terreforts » et aux sols légers et profonds des "boulbènes". Chaque communauté agricole distinguait ainsi son causse, par exemple le causse de Caylus, le causse de Limogne ou le causse de Cajarc. C'est par extension que l'appellation Causse de Limogne désigne tout un petit pays. La présence des poches à phosphate déborde un peu vers le Nord la vallée du Lot, et vers l'Est le Causse de Limogne proprement dit (Causse de Villeneuve).   

Record of life and works of Henri Menu, French zoologist, contributor to the knowledge of living and fossil bats. 

The present study of Artiodactyla from the Middle Eocene of the Geiseltal lignite beds concems systematics, biostratigraphy, and palaeoecology on the basis of 174 specimens: isolated remains to more complete skeletons. Instead of the formerly known five species of two families are now recognized 14 species of the Diacodexeidae, Dichobunidae, Cebochoeridae, and Haplobunodontidae. New species are Aumelasia maniai, Anthracobunodon neumarkensis, Masillabune franzeni. Four species of the Geiseltalfauna are definitely known from elswere, and five species are closely related to those from other European localities. Evidently the faunal situation of artiodactyls during the Middle Eocene of Europe was largely uniform. The distribution of artiodactyls within the sequence of the Geiseltal strata corroborates the biostratigraphical concept of the land mammal age Geiseltalian (Franzen & Haubold l986b) as well as the mammalian reference levels MP 11-13 (Franzen 1987). Reconstructions of the skulls and skeletons allow conclusions on the functional morphology and palaeoecology of the artiodactyls of the European Middle Eocene 

More than 400 paleontological type-specimens housed in the Montpellier University collections have been inventoried in this catalogue which includes charophytes, Paleozoic plants, brachiopodes, molluscs, arthropodes and vertebrates (selachians, amphibians, reptiles, birds and mammals). The vertebrates have been treated exhaustively in the catalogue and one can consider that it includes most of the type specimens deposited in the Montpelier II collections. 

The dentitions as well as one complete and several partial skeletons of Equoids from the Eocene lignite beds of the Geiseltal locality are revised. Instead of 13 species distinguished up to now 3 chronoclines with 5 species and 3 separate species are recognized (text. fig. 1). Propalaeotherium hassiacum HAUPT, 1925 is evolving into Propalaeotherium isselanum (CUVIER, 1824) between the levels of the « obere Unterkohle ›› and the « untere Mittelkohle ›› of the Geiseltal section. Propalaeotherium argentonicum GERVAIS, 1849 is shown to be present in the « untere Unterkohle ››, whereas Lophiotherium pygmaeum (DEPERET,1901) occurs in the « obere Mittelkohle ›› and in the « oberes Hauptmittel ››. Plagiolophus cartieri STEHLIN, 1904 appears during the transition from the « Mittelkohle ›› into the « Oberkohle ›› as the earliest true Palaeothere. Therefore the « Oberkohle ›› is already regarded as Upper Eocene. This is corroborated by the occurrence of a phyletic descendant of Propalaeatherium parvulum (Propalaeotherium n.sp.) in the middle and upper "Oberkohle " because this species appears otherwise for the first time at the mammal level of Lissieu. On the other hand Propachynolophus gaudryz (LEMOINE, 1878) described by Matthes (1977) from the « untere Unterkohle ›› turns out te be in fact a Phenacodont. Thus the decisive argument for classifying the « untere Unterkohle ›› as Lower Eocene has to be dropped. Biostratigraphically the « Unterkohle ›› and the «Basishauptrnittel ›› correspond with the lower Middle Eocene (mammal level of Messel), whereas the «unteres Hauptmittel ›› and the « untere Mittelkohle ›› are equivalent to the middle part of the middle Eocene (mammal level of lssel), and the « obere Mittelkohle ›› together with the « oberes Hauptmittel ›› coincide with the upper Middle Eocene (mammal level of Bouxwiller). 

Tarsals that can be confidently attributed to Paschatheríum dolloi from Dormaal (Belgium) are described. The astragalus is short; its broad neck is set at an angle of 30 degrees to the trochlea. The trochlea is pulley-shaped and proximally extended. There is no astragalar foramen. The medial tibial facet extends distally in a cup deeply excavated in the neck and buttressed. The sustentacular facet extends toward the navicular facet but is not fully confluent with it. The calcaneum bears a proximo-distally extended proximal facet for the astragalus. A relatively large peroneal tubercle projects from the body, and is situated distally. Functionally, the trochlea indicates extensive flexion-extension movements of the foot. Calcaneo-astragalar facets indicate sliding and rotation between the two tarsals. The inclination of the navicular facet suggests frequent foot inversion. The peroneal tubercle reflects good muscular capacities for foot rotation. Overall morphology is interpreted as a scansorial adaptation similar to that of sciurids.Comparisons are made with the tarsals of Macrocranion vandebroeki from Dormaal and Hyopsodus paulus from the Bridgerian of Wyoming. Some similarities between the astragali of Paschatherium and Macrocraníon (trochlea) are interpreted as convergences for rapid locomotion. However absence of mobility at the lower ankle and midtarsal joints in M. vandebroekzi suggests that this species was cursorial, as is known for M. tenerum from Messel. Similarities in the calcanea of Paschatherium and Hyopsodus are probably the result of close phylogenetic relations, and confirm the placement of Paschatherium in the hyopsodontids. The differences in the calcanea of Paschatherium and Macrocranion underline that Paschatherium is distinct from erinaceomorph insectivores. The differences in astragalar morphology between Paschatherium and Hyopsodus show that a marked adaptive divergence separates the two genera. We speculate about the common occurrence of a deep tibial cup (“cotylar fossa”) and a pulley-shaped trochlea in Paschatherium and hyracoids, suggesting that an adaptive scenario similar to that having led to Paschatherium (scansoriality) might explain the acquisition of the peculiar hyracoid tarsal characters; such a scenario contradicts the concept of Pantomesaxonia. Other peculiar characters of Hyopsodus suggest that hyopsodontids might be given more consideration in the search for hyracoid (and tethythere) origins. 

Simpson (1937a) reconstructed the brain of the Paleocene multituberculate Ptilodus as having the olfactory bulbs widest anteriorly, an unusual condition among mammals. Slight preparation and reexamination of the endocast specimens of Ptilodus reveals that the olfactory bulbs in fact taper anteriorly, as in the recently-described endocranial casts of three multituberculate species from the Late Cretaceous of Asia, and as in those of other mammals. The brain of Ptilodus was therefore essentially of the same general pattem as in other multituberculates. Ptilodus differs, however, in having the vermis more deeply inserted between the cerebral hemispheres. Other details concerning the endocast morphology of Ptilodus are clarified.

The encephalization quotient (EQ) of Ptilodus is recalculated from revised estimates of both endocranial volume and body mass to fall somewhere within a broad range of values; from 0.41 to 0.62 if the olfactory bulbs are included and from 0.37 to 0.55 if they are not. In any case, the relative brain size of Ptilodus is roughly equivalent to that of Chulsanbaatar, the only other multituberculate for which EQ has been calculated, but considerably smaller than that of an average extant mammnal. 

The fossil mammals collected from the Eocene of Hammada du Dra (northwest Sahara. Algeria) and two fragmentary teeth from the Lutetian of M'Bodione Dadere (Senegal) are described.
The fossils from the northwest Sahara come from a lacustrian deposit dated by charophytes (Raskyella aff. pecki, Raskyella n. sp.. Maedleriella lavocati, Maedleriella sp. et ? Peckichara sp.) as Middle Eocene or perhaps Lower Eocene (Gevin, Feist and Mongereau, 1974). Several hyracoids (3 or 4) identified from this formation extends the age of the family Pliohyracidae Osborn in Africa. Three forms appear to belong in the genera Megalohyrax, Titanohyrax and perhaps Bunohyrax which have been know until now only from the lower Oligocene of the Fayum (M. gevini n. sp. ; T. mongereaui n. sp.. ? Bunohyrax or Megalohyrax indet.). Another hyracoidof small size is referred to a new genus, Microhyrax (M. lavocati n. sp.).
Helioseus insolitus n. g. n. sp. is described without ordinal assignment. Azibius (Sudre, 1975) which has been the subject of questions and interpretations is reviewed.
Only one tooth from the Lutetian of M'Bodione Dadere is complete enough to interpret. lt probably belongs to a condylarth and demonstrates for the first time, the presence of the order in Africa. The second tooth is too fragmentary for comment.
In conclusion., the paleobiogeographic role of Africa at the end of the cretaceous and the beginning of the Cenozoic is discussed. 

The late Pliocene site (MN 16) of Balaruc II (Hérault, France) has provided remains of the following amphibians and reptiles: Chelotriton pliocenicus nov. sp. and Triturus marmoratus (Salamandridae), cf. Rana (Ranidae), cf. Blanus (Amphisbaenidae), cf. Agama (Agamidae),  Gekkonidae indet., Lacerta s.l. (Lacertidae), "Ophisaurus" sp. (Anguidae), Michauxophis occitanus (Aniliidae), Erycinae indet. (Boidae), Elaphe cf. E. longissima and Malpolon sp. (Colubridae), cf. Naja (Elapidae) and Vipera sp. (Viperidae). The salamandrid Chelotriton pliocenicus and the aniliid Michauxophis occitanus constitute, up to now, the only records of these groups in the European Pliocene. The fauna is indicative of a warm, dry
subtropical climate. 

Many types of insectivores have been described from specimens found in the Quercy phosphorites. These remains very often were not dated because they came from old collections. Recent excavations have permitted the situation of Amphidozotherium cayluxi FILHOL in the late Eocene. Two new genera are descrlbed based on material both from the old collections (Cryplotopos nov. g.) and from that recently recovered (Darbonetus nov. g., beginning of the middle Oligocene). Their systematic positions are revised and comparisons with American faunas are made. Amphidozotherium is not a talpid, but an erinaceoid belonging to an indeterminate family. Saturninia gracilis STHELIN is classified among the Nyctitheriinae, Myxomygale antiqua FILHOL among the Urotrichini Talpinae, and the genus Geotypus POMEL among the Scaptonichini Talpinae. A new study of the talpids from Auvergne has been rendered necessary. During the late Eocene and Oligocene precise morphology relationships existed between certain insectivores of Europe and North America. 

The fauna from three new rodent localities (Castelmaurou, Grépiac-carrière et Grépiac-rive gauche) from Oligo-Miocene molasses of the Toulouse area is described. The one from Colomiers is completed. 11 species belonging to 4 families (Cricetidae, Eomyidae, Gliridae, Sciuridae) are present. The Miocene localities of Grépiac-carrière and Colomiers are correlated with Balizac, La Brète, Lambert and Lespignan. Grépiac-rive gauche is just a little older than these sites. Castelmaurou is somewhat younger than La Milloque and belongs to Oligocene. 

 A new genus of hystricognath rodent with two new species, Soriamys gaimanensis and Soriamys ganganensis, from the Colhuehuapian Age (Early Miocene), Sarmiento Formation, of Patagonia is described. The first species comes from the south barranca of the valley of Rio Chubut, near Gaiman locality (Chubut Province). It is known through a great number of dental remains in different stages of wear. The teeth are protohypsodont, with cement in the principal valleys. P4 are simpler, more oval inoutline and without a differentiated hypocone-hypoflexus. Upper molars are pentalophodont in early stages of wear and become bilobated in middle and advanced stages; M3 have a temporary third posterior lobe due to the maintenance of the braquiflexus on the posterior wall of the tooth. Lower teeth have a completely asymrnetrical pattern in relation to the uppers. The molars are trilophodont, with only one complex crest in the trigonid composed of the fusion of the anterolophid and mesolophid. The dp4 have a derived pentalophodont pattern due to the loss or fusion of the mesolophid and the development of an accessory transverse crest between the anterolophid and metalophid. The second species is known through a complete skull and jaw and other skull fragments with the dentition, proceeding from Pampa de Gan Gan, Chubut province. Respect to the first species, the teeth are higher crowned, with an earlier occlusal simplification and a third posterior lobe of M3 more developed and persistent. The skull and jaws show many chinchilloid characters, such as jugal bone with an ascending process, concave palate, very prominent dorsal shelf of the masseteric fossa, nasolachrymal duct opened laterally on the maxillary and very developed lateral mandibular fossa. Moreover, Soriamys is closely related to Cephalomys by sharing a similar asymmetric dental pattern and other dental and mandibular characters. These two genera constitute a natural group, the Cephalomyidae, with peculiar dental characters, like the asymmetric pattem of the upper and lower teeth; Cephalomyopsis, and probably Litadontomys, can be considered part of this group. Scotamys and Perimys constitute a distinct lineage (the Neopiblemidae or Perimyidae), more closely related to the chinchillids. Many characters shared by cephalomyids, eocardiids and caviids suggest a closer affinity between the Chinchilloidea and the Cavioiidea as a whole. Abrocoma shows also an asymmetric dental pattern and other chinchilloid features that suggest some degree of relationship with the cephalomyids, still not well determined. 

Seventeen species of cricetid rodent are recognized and described from lower and middle Siwalik deposits in the Potwar Plateau of Pakistan. These species are grouped in three categories, characterized as subfamilies (e. g., Megacricetodontinae, Myocricetodontinae, and Dendromurinae); an additional and more abundant category of rodents from these deposits, the Democricetodontinae, is excluded from this study, and will be described in a later study. Fifteen of the species are new, and four new genera are described. The Siwalik cricetid taxa are : Megacricetodon aquilari, n. sp.; Megacricetodon sivalensis, n. sp.; Megacricetodon daamsi, n. sp.; Megacricetodon mythikos, n. sp.; Punjabemys downsi, n. gen. & n. sp.; Punjabemys leptos, n. gen. & n. sp.; Punjabemys mikros, n. gen. & n. sp.; Myocricetodon sivalensis, n. sp.;  Myocricetodon sp.; Dakkamyoides lavocati, n. gen. & n. sp.; Dakkamyoides perplexus, n. gen. & n. sp.; Dakkamys asiaticus, n. sp.; Dakkamys barryi, n. sp.; Dakkamys sp.; Paradakkamys chinjiensis, n. gen. & n. sp.; Potwarmus primitivus, n. gen.; and Potwarmus minimus, n. gen. & n. sp. This diverse record of middle Miocene small mammals illuminates a profound radiation of cricetid rodents in southem Asia, the effects of which were felt in Europe and Africa as well as the rest of Asia. 

The knowledge of the Anchilophini has been lately renewed by the discovery of a rather large amount of new material still largely unpublished. This new material offers the opportunity of a systematic revision of this tribe gathering those of European Eocene Equoidea which bear no mesostyle on upper check teeth and display a heavy trend to the molarization of premolars.

A cladistic analysis has made out two genera, Anchilophus (Paranchilophus included as a subgenus), characterized by a marked lophodonty and the transverse narrowness of the cheek teeth, a rather high hypsodonty, the frequent occurrence of "crochets" and "anticrochets" on the superior ones, and a rather weak molarization of the premolars, opposite to Metanchilophus n. gen. whose cheek teeth are more transversally elongated, less high, less lophodont, with cusps better distinct, enamel thicker and premolars more molarized on the whole.

Three species of Anchilophus are recognized, A. desmaresti, type species of the genus, A. (Paranchilophus) remyi and A. (Paranchilophus) jeanteli n. sp.

The genus Metanchilophus is more diversified with the species dumasi, radegondensis, gaudini (whose a new sub-species M. g. fontensis is defined), depereli, castrensis n. sp. and chaubeti n. sp.

The skull anatomy has been moreover described with several taxa; it brings to light (for all that one can generalize) that Anchilophini were light animals with a slender and elongated snout, a thin zygomatic arch, a rather developed encephalon with an advanced gyrencephaly.

The structure of the nasal opening together with the occurrence of epitympanic sinuses and the molarizing process of the premolars corroborate the attribution of this tribe to the family PalaeotheIiidae. 

Revision of the hipparion material from Montredon, including newly excavated and other unpublished specimens brings evidence of specific heterogeneity.
A fragmentary very small MC III seems very close to H. macedonicum from the upper Vallesian of Ravin de la Pluie, Greece. In that same site was also found a large hipparion.
Most of the Montredon material is referred to H. depereti. This species associates characters usually found in Vallesian hipparions (highly plicated upper cheek teeth, deep vestíbular grooves on the lower cheek teeth, robust metapodials) with characters more frequent in Turolian forms (middle size, lack of confluence in the upper premolar fossettes, lack of ectostylids on the adult lower cheek teeth, well developped keel on the MC III, facette for the 2nd cuneiform present on all MT III). H. depereti shares some of these characters with the Spanish and Portuguese hipparions transítional between the Vallesian and the Turolian (Masia del Barbo, Azambujeira) but is not identícal to any of them. The upper Vallesian hipparion material from Diavata, Greece, probably belongs to H. depereti but not the large hipparion rests from Ravin de la Pluie.
Thus, Montredon and Ravin de la Pluie may well share the same small species, H. macedonicum, but they differ in the associated one: middle-sized H. depereti at Montredon, large-sized H. primigenium at Ravin de la Pluie. Both sites, however, give evidence of small hipparions during the Vallesian, coexisting with other larger species.
The present paper also proposes an adaptation of the Kiesewalter's indices that calculates the height at the withers using the metapodial length, and discusses indices proposed by Gromova and by Sen et al. to express the relative development of the metapodial keel. 

The genus Parasteiromys AMEGHINO, 1904 is revalidated, and P. friantae sp. nov. (Hystricognathi, Erethizontidae) from Colhuehuapian (early Miocene) sediments of the southern cliff of Colhue-Huapi Lake (Province of Chubut, Argentina), is described. The molar morphology of these taxa and of living porcupines adds new elements to understand the dental evolution of the Erethizontidae, and to propose the hypothetical ancestral molar pattern for this family. This pattern does not correspond to any of the morphologies traditionally proposed as ancestral for South American hystricognathous rodents. The proposed pattern is characterized by a metaloph disconnected from the posteroloph and oriented towards the hypocone, and the third loph incompletely developed with the lingual portion homologous to the mesolophule of Baluchimyinae (Chapattimyidae) from the Miocene of Pakistan. The inferred steps of the molar evolution of erethizontids towards the pentalophodont condition, considered derived for the family, are illustrated. This study strengthens the hypothesis placing erethizontids in a basal position among rodents of the suborder Hystricognathi.

  

The hipparions from the Dytiko localities of the lower Axios valley (Macedonia, Greece) are studied. The material comes from three localities Dytiko-l, 2, 3 (DTK, DIT, DKO), which are situated near the village of Dytiko, about 60 km northwest to Thessaloniki. Three species have been determined, the medium-sized H. mediterraneum, the small-sized H. matthewi and the very small-sized H. periafricanum. The determined Hipparion species, their morphological characters and their comparison with the other Axios valley material indicate a Late Turolian age for the Dytiko localities.